Forbes D P, Steffek A J
Department of Orthodontics, Northwestern University Dental School, Chicago, IL 60611.
J Craniofac Genet Dev Biol. 1989;9(4):367-80.
Previously, Forbes et al. [J Craniofac Genet Dev. Biol, 9:271-284, 1989] and Millicovsky et al. [Am J Anat 164:29-44, 1982], demonstrated that some of the epithelial cells of the primary palate formed extensive projections, bridging the medial and lateral nasal prominences. These connections are thought to aide in the fusion process by facilitating union of the prominences, a process known as secondary fusion [Millicovsky et al., 1982]. In order to study the epithelial cell and its behavior more closely an in vitro model was established [Gibson et al.: J Craniofac Genet Dev Biol, 1989], where epithelial cells in culture were shown to produce many of the morphologic characteristics observed in vivo. In the present study, an in vitro model is discussed which reproduces the epithelial projections observed in vivo. Epithelial cells, previously characterized, were obtained from the primary palate of 13-day-old rat embryos and sub-cultured as explants. Comparisons were made with the epithelial bridging observed in vivo of two species of animals. The results indicated sub-cultured epithelium as isolated cells, at either low or high density, rarely formed bridges. Primary cultures of epithelial explants also infrequently formed projections. However, sub-cultures of epithelial explants, plated as small clusters of cells with intervening spaces between cell groups, demonstrated extensive epithelial bridging. Epithelial projections did not form from cells that were directly attached to the plastic culture dish; only superficial, elevated cells formed projections. Significantly, the connections that occurred between explants did not attach to the plastic substratum. Instead, they appeared as line connections suspended by the medium. With time, the number of projections increased and epithelial cells could be seen along the projections forming an epithelial bridge. This study established a model of epithelial bridging in vitro for analysis of a process which has been shown to be an integral part of primary palate fusion.
此前,福布斯等人[《颅面遗传与发育生物学杂志》,9:271 - 284,1989年]以及米利科夫斯基等人[《美国解剖学杂志》164:29 - 44,1982年]证明,原发腭的一些上皮细胞形成了广泛的突起,连接内侧和外侧鼻突。这些连接被认为通过促进鼻突的结合来辅助融合过程,这一过程被称为二次融合[米利科夫斯基等人,1982年]。为了更密切地研究上皮细胞及其行为,建立了一个体外模型[吉布森等人:《颅面遗传与发育生物学杂志》,1989年],其中培养的上皮细胞表现出许多在体内观察到的形态学特征。在本研究中,讨论了一个体外模型,该模型重现了在体内观察到的上皮突起。先前已鉴定的上皮细胞取自13日龄大鼠胚胎的原发腭,并作为外植体进行传代培养。对两种动物体内观察到的上皮桥接进行了比较。结果表明,作为分离细胞的传代培养上皮,无论低密度还是高密度,很少形成桥接。上皮外植体的原代培养也很少形成突起。然而,作为小细胞簇接种且细胞群之间有间隔的上皮外植体传代培养,显示出广泛的上皮桥接。上皮突起并非由直接附着在塑料培养皿上的细胞形成;只有表面隆起的细胞形成突起。值得注意的是,外植体之间形成的连接并未附着在塑料基质上。相反,它们表现为被培养基悬浮的线状连接。随着时间的推移,突起数量增加,并且可以看到沿突起有上皮细胞形成上皮桥。本研究建立了一个体外上皮桥接模型,用于分析一个已被证明是原发腭融合不可或缺部分的过程。